EP3717439A1 - Procédé de synthèse pour la préparation d'un matériau contenant du zirconate de calcium ainsi que remblai et produit réfractaire céramique grossier pourvu d'un produit en grains présynthétisé contenant du zirconate calcium - Google Patents

Procédé de synthèse pour la préparation d'un matériau contenant du zirconate de calcium ainsi que remblai et produit réfractaire céramique grossier pourvu d'un produit en grains présynthétisé contenant du zirconate calcium

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Publication number
EP3717439A1
EP3717439A1 EP18812125.5A EP18812125A EP3717439A1 EP 3717439 A1 EP3717439 A1 EP 3717439A1 EP 18812125 A EP18812125 A EP 18812125A EP 3717439 A1 EP3717439 A1 EP 3717439A1
Authority
EP
European Patent Office
Prior art keywords
raw material
synthesis method
material component
grain
din
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
EP18812125.5A
Other languages
German (de)
English (en)
Inventor
Helge Jansen
Christos Georgios ANEZIRIS
Constantin JAHN
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Refratechnik Holding GmbH
Original Assignee
Refratechnik Holding GmbH
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Refratechnik Holding GmbH filed Critical Refratechnik Holding GmbH
Publication of EP3717439A1 publication Critical patent/EP3717439A1/fr
Pending legal-status Critical Current

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    • C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/66—Monolithic refractories or refractory mortars, including those whether or not containing clay
    • C—CHEMISTRY; METALLURGY
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    • C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
    • C04B35/48—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on zirconium or hafnium oxides, zirconates, zircon or hafnates
    • C04B35/482—Refractories from grain sized mixtures
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    • C01—INORGANIC CHEMISTRY
    • C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G25/00—Compounds of zirconium
    • C01G25/006—Compounds containing, besides zirconium, two or more other elements, with the exception of oxygen or hydrogen
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B22—CASTING; POWDER METALLURGY
    • B22D—CASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
    • B22D41/00—Casting melt-holding vessels, e.g. ladles, tundishes, cups or the like
    • B22D41/02—Linings
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B22—CASTING; POWDER METALLURGY
    • B22D—CASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
    • B22D41/00—Casting melt-holding vessels, e.g. ladles, tundishes, cups or the like
    • B22D41/14—Closures
    • B22D41/22—Closures sliding-gate type, i.e. having a fixed plate and a movable plate in sliding contact with each other for selective registry of their openings
    • B22D41/28—Plates therefor
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    • C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
    • C04B35/48—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on zirconium or hafnium oxides, zirconates, zircon or hafnates
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    • C04B35/62605—Treating the starting powders individually or as mixtures
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    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
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    • F27—FURNACES; KILNS; OVENS; RETORTS
    • F27B—FURNACES, KILNS, OVENS, OR RETORTS IN GENERAL; OPEN SINTERING OR LIKE APPARATUS
    • F27B14/00—Crucible or pot furnaces
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    • F27B14/10—Crucibles
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    • F27D—DETAILS OR ACCESSORIES OF FURNACES, KILNS, OVENS, OR RETORTS, IN SO FAR AS THEY ARE OF KINDS OCCURRING IN MORE THAN ONE KIND OF FURNACE
    • F27D1/00—Casings; Linings; Walls; Roofs
    • F27D1/0003—Linings or walls
    • F27D1/0006—Linings or walls formed from bricks or layers with a particular composition or specific characteristics
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
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    • F27D—DETAILS OR ACCESSORIES OF FURNACES, KILNS, OVENS, OR RETORTS, IN SO FAR AS THEY ARE OF KINDS OCCURRING IN MORE THAN ONE KIND OF FURNACE
    • F27D1/00—Casings; Linings; Walls; Roofs
    • F27D1/0003—Linings or walls
    • F27D1/0033—Linings or walls comprising heat shields, e.g. heat shieldsd
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    • C04B2235/30—Constituents and secondary phases not being of a fibrous nature
    • C04B2235/32—Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3205—Alkaline earth oxides or oxide forming salts thereof, e.g. beryllium oxide
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Definitions

  • the present invention relates to a synthesis method for producing a refractory oxide ceramic material from CaZrCb, in particular in the form of a refractory, preferably mechanically comminuted, in particular crushed and / or ground, grain size, and an offset and a coarse ceramic shaped or unshaped refractory product containing at least one vorsynthetflowere calciumzirkonatumble fireproof grit.
  • refractory should not be limited within the scope of the invention to the definition according to ISO 836 or DIN 51060, which define a cone falling point of> 1500 ° C.
  • Refractory products according to the invention have a printer softening point To, 5 according to DIN EN ISO 1893: 2009-09 of TO, 5 ⁇ 600 ° C, preferably To, 5 ⁇ 800 ° C.
  • refractory or refractory granular materials or grains within the meaning of the invention are those materials or grains which are suitable for a refractory product with the above-mentioned printer softening point To , 5 .
  • the refractory products of the invention are used to protect aggregate structures in aggregates in which temperatures between 600 and 2000 ° C, in particular between 1000 and 1800 ° C prevail.
  • heavy clay products are products that are produced from grain sizes with grain sizes up to 6 mm, in special cases also up to 25 mm (see “Gerald Routschka / Hartmut Wuthnow, Practical Guide” Refractory Materials “, 5th edition, Vulkan-Verlag, (hereinafter only with “practice handbook” designated, chapter 2).
  • grain or "granular material” in the context of the invention comprises a pourable solid which consists of many small, solid grains. If the grains have a particle size ⁇ 200 pm, they are the grain around a flour or powder. If the grains are produced by mechanical comminution, eg breaking and / or grinding, this is a crushed granulate or a broken granulation. Granulation may, however, also include granules or granules of pellets produced by granulation or pelleting without mechanical comminution.
  • Grain distribution of grain is usually adjusted by sieving.
  • Shaped coarse ceramic products are unfired, tempered or ceramically fired, preferably manufactured in a ceramic factory, especially stones or plates. They have a defined geometry and are ready to be installed. The shaping takes place e.g. by pressing, pounding, ramming or slip casting. The molded products, in particular the stones, are e.g. for the formation of a delivery, with mortar or mortar-free (“crunchy") walls.
  • the shaping takes place e.g. by pressing, pounding, ramming or slip casting.
  • the molded products, in particular the stones are e.g. for the formation of a delivery, with mortar or mortar-free (“crunchy") walls.
  • the unshaped articles of the invention are products which, for the most part by the user, are formed from an unshaped mass or batches, eg by casting, vibrating, poking, pounding or spraying. Unformed products are usually placed at the place of use behind formwork in larger fields and Form after hardening part of the delivery. For example, the unshaped products are sprayed masses, ramming masses, castables, vibrating masses or casting compounds.
  • Both the shaped and unshaped products according to the invention are produced in a manner known per se from a coarse ceramic offset.
  • Calcium zirconate is the stable stoichiometric composition in the phase diagram CaO-ZrCh. It has a high melting temperature of 2368 ° C and is resistant to alkali corrosion. Since it is rarely found as a mineral in nature, calcium zirconate has to be synthesized for technical applications. In this presynthesis, the goal is to produce a phase-pure material or a material of 100% calcium zirconate. Because this ensures good properties of the refractory products produced from the presynthesized material.
  • DE 10 2012 003 483 discloses a thermal shock and corrosion resistant ceramic product based on calcium zirconate, wherein the structure of the product consists of pre-synthesized calciumzirconate-containing crushed granules.
  • the crushed granules have a Zr0 2 / CaO ratio between 1.6: 1 and 1: 1.5, and a particle size of 100 pm to 6 mm.
  • the crushed granules have a share of> 50 wt .-%.
  • the product has a binding matrix of fine-grained calcium zirconate and / or zirconium dioxide surrounding the crushed granules and sintered at> 1300 ° C., with grain sizes between 50 nm and 150 ⁇ m.
  • the calciumzirconate-containing crushed granules may be a sintered and crushed crushed granules based on synthesized CaZrO 3 from CaCO 3 and ZrO 2 , wherein the sintered crushed granules have been sintered at temperatures above 1300 ° C.
  • the binding matrix can be prepared from a mixture of calcium carbonate with a particle size of 50 nm to 150 gm and unstabilized zirconium dioxide with a particle size between 50 nm and 150 gm.
  • the crushed granules are also preferably produced by slip casting technology. It can also be produced by sculptural molding or press technology.
  • DE 10 2012 003 478 A1 deals with the use of an oxide-ceramic material which has at least 75% by weight of CaZrCb and at most 25% by weight of ZrO 2 as lining material for coal gasification plants.
  • the production of the material takes place for example via slip casting technology.
  • Zr ⁇ 2 mixed with CaCCb and other additives and processed with the addition of water to a slurry.
  • the molar ZrO 2 / CaCO 3 ratio is between 1.6: 1 and 1: 1.5.
  • the slurry is poured into a plaster mold, which withdraws the water from the slurry again, so that moldings are obtained.
  • the shaped bodies are dried and then sintered at temperatures between 800 and 1700 ° C., preferably at 1300 to 1500 ° C., under oxidizing or reducing conditions.
  • the slip-molded test specimens of CaZrCb are broken into different particle classes and the grain size is processed to give a castable or vibratable mass using further additives.
  • This mass which consists of coarse and fine-grained CaZrCb and small amounts of Zr ⁇ 2 , is then dried and sintered.
  • DE 10 2012 003 478 A1 such large-sized components with an open porosity of up to 20% can be produced.
  • an embodiment is also included, in which the material obtained after sintering at 1400 ° C 64% CaZrCb and 36% Cao.isZro.ssOi.ss.
  • Object of the present invention is to provide a simple and inexpensive, economical and environmentally safe method for the synthesis of a preferably phase-pure, calcium zirconate material, preferably in the form of a calciumzirkonat conveniencen grain.
  • Another object is to provide an offset for producing a coarse ceramic, unshaped or formed refractory product having at least one such synthesized calcium zirconate containing grain and such a heavy clay refractory product.
  • FIG. 1 shows an X-ray phase diagram of a device according to the invention according to FIG. 1
  • Embodiment 1 grain produced from phase-pure Ca le mezukonkontechnikstoff FIG. 2 an X-ray phase diagram of a molded article produced according to the invention in accordance with exemplary embodiment 2
  • a, preferably phase-pure, calciumzirconate-containing material by means of compression molding and sintering from a mixture consisting exclusively of at least one Ca-containing flour-like raw material component, at least one ZrCh-containing flour-shaped raw material component and water and a water content of> 5 to 10 wt .-%, preferably 7 to 8 wt .-% water based on the dry mass of the mixture.
  • the synthesis process according to the invention thus has the following process steps: a) Preparation of the mixture of the at least one Ca-containing flour-like raw material component containing at least one Zr ⁇ 2- containing flour-like raw material component and the water with a water content of> 5 to 10 wt .-%, preferably 7 to 8% by weight of water based on the dry mass of the mixture, b) pressing the mixture into a green shaped body,
  • the mixture thus contains a higher proportion of water than is customary in conventional press molding.
  • the mixture according to the invention contains no further constituents, in particular no binders and / or pressing aids.
  • the binders and / or pressing aids change the previously set molar ratio CaO / ZrCh during firing. It is believed that the organic binders and / or pressing aids release CO and / or CO 2 during firing, which reduces the Ca contained in the raw materials. The reduced Ca in turn passes into a gas phase and evaporates, so that the molar ratio Ca0 / Zr0 2 changes. These reactions take place from a temperature of about 550 ° C. Thus, the synthesis is disturbed by the organic binder and / or pressing aids, even if they are present only in very small amounts, in particular so that the production of a phase-pure material is not possible.
  • the high water content according to the invention ensures sufficient cohesion of the green shaped body, even without a binder. Furthermore, it has surprisingly been found that the high water content in the mixture also contributes to the fact that a phase-pure material can be produced. Because of the high water content prevails in the sintering process, a water vapor atmosphere, which supports the sintering process. The water vapor atmosphere reduces the surface tension of the individual flour grains of the raw materials, which improves the sinterability. In addition, the effect
  • the molar ratio Ca0 / Zr0 2 in the mixture should be substantially equimolar. That is, the molar ratio Ca0 / Zr0 2 in the mixture is preferably 1: 1. However, at least the molar ratio is preferably 1: 5: 1 to 1: 1, 6. In the determination of the molar ratio is idealized in each case from a pure raw material. Starting from the desired ratio is calculated on the molar masses, the weight ratio. Of course, it is taken into account that the CaO carriers also contain other constituents, for example CCh, in the CaCCb.
  • the Ca raw material component used is preferably a CaCCb and / or CaO and / or Ca (OH) 2 and / or CaC 2 -containing raw material component.
  • a CaCO 3 raw material component is used.
  • the CaCO 3 raw material component is preferably natural, ground limestone meal (GCC) or synthetic, precipitated calcium carbonate (PCC) or chalk. Especially preferred, especially because of its high purity, is PCC.
  • the preparation of PCC is preferably carried out by reaction of carbon dioxide with lime or a hydrated lime suspension.
  • the hydrated lime suspension is prepared either by quenching quicklime or by dispersing calcium hydroxide in water.
  • the CaO raw material component is preferably quicklime.
  • the Ca (OH) 2 raw material component hydrated lime is preferably used.
  • the ZrO 2 raw material component it is preferable to use synthetic zirconia.
  • the zirconia is not stabilized (monoclinic). But it can also be stabilized.
  • each of the raw material components preferably has a purity of at least 96% by weight, preferably at least 99% by weight.
  • the minimum content of the particular compound (CaCO 3, CaO, Ca (OH) 2 , CaC 2 or ZrO 2 ) is preferably at least 96% by weight, preferably at least 99% by weight, determined in each case by X-ray fluorescence analysis (RFA) according to DIN 51001: 2003.
  • the Ca raw material component has a particle size of ⁇ 200 pm, preferably of ⁇ 50 pm, more preferably between 200 nm and 10 pm in accordance with DIN EN 725-5: 2007.
  • the mean grain diameter of the Ca raw material component is preferably 500 nm to 5 ⁇ m, preferably 0.8 to 1 ⁇ m.
  • the ZrCh raw material component preferably has a particle size of ⁇ 200 pm, preferably of ⁇ 150 pm, more preferably between 200 nm and 10 pm in accordance with DIN EN 725-5: 2007.
  • the average grain diameter (dso) of the ZrCh raw material component is preferably 500 nm to 5 ⁇ m, preferably 0.7 to 1 ⁇ m.
  • the grain sizes and the average grain diameter are determined by means of laser granulometry according to DIN EN 725-5: 2007.
  • the respective flour is preferably dispersed by means of ultrasound, preferably in ethanol.
  • the shaping of the mixture consisting exclusively of the raw material components and of water into green shaped bodies takes place according to the invention by pressing.
  • the pressing is preferably carried out at a pressure of 30 to 150 N / mm 2 , preferably from 50 to 80 N / mm 2 .
  • the pressing is preferably carried out by uniaxial pressing. But it can also be done by isostatic pressing or vibratory pressing or briquetting or pelleting.
  • the mixing preferably takes place in the intensive mixer in a countercurrent process (turbulence and plate rotate in opposite directions).
  • the green pressed molded bodies preferably have the following dimensions:
  • the green shaped bodies also preferably have a bulk density determined according to DIN EN 993-17: 1999 of 2.0 to 3.0 g / cm 3 , preferably 2.1 to 2.5 g / cm 3 , and / or a porosity according to DIN 66133: 1993-06 from 30 to 60% by volume, preferably 40 to 50% by volume.
  • they preferably have a cold bending strength according to DIN EN 993-6: 1995-04 of at least 1 MPa.
  • the green moldings After pressing, the green moldings, as already explained, dried.
  • the drying is preferably carried out to a residual moisture content of between 0 and 2% by weight, in particular between 0 and 0.5% by weight, determined in accordance with DIN 51078: 2002-12.
  • the green shaped bodies are preferably dried between 25 and 110 ° C., in particular between 100 and 105 ° C., for a time of 4 to 24 hours, preferably 12 to 24 hours.
  • the sintering takes place according to the invention.
  • the sintering is preferably carried out with a holding phase at a final temperature of 1200 to 1800 ° C, preferably 1400 to 1650 ° C, for a period of 2 to 10 hours, preferably from 4 to 6 hours.
  • it is heated at a heating rate of 1 to 10 K / min, preferably from 2 to 5 K / min.
  • an intermediate holding phase at a temperature of 400 to 1000 ° C, preferably 550 to 900 ° C, for a period of 1 to 3 hours, preferably from 1, 5 to 2.5 hours performed.
  • the cooling preferably takes place freely in the oven.
  • the sintering is preferably carried out under neutral or oxidizing conditions.
  • the sintering is also preferably carried out in an electrically heated or a gas-fired furnace.
  • Gas-fired furnaces have a controllable oxygen content in the combustion air (oxygen overflow or under-run), can reach higher heating rates and usually have a (different) flow field of the gases in the combustion chamber compared to electrically heated furnaces.
  • the sintering takes place in a discontinuous or continuous process, industrially preferably in a continuous process.
  • phase-pure calcium zirconium material As already explained, it is possible in particular with the method according to the invention to produce a very pure, in particular a phase-pure, calcium zirconium material.
  • the phase-pure calcium zirconium material produced according to the invention thus has no free raw materials and no mixed phases, in particular. So there has been a complete implementation of the raw material components used to calcium zirconate.
  • At least the calcium zirconium material produced according to the invention has a content of at least 98% by weight, preferably at least 99% by weight, of CaZrO 3, based on the dry mass of the calcium zirconium material.
  • FIG. 1 An exemplary X-ray phase diagram of a phase-pure calcium zirconium material produced according to the invention in accordance with the exemplary embodiment is shown in FIG.
  • the phase analysis takes place according to DIN 13925-2: 2003.
  • the dried, ground substance ( ⁇ 45 pm) is prepared in the sample carrier.
  • the testing device is preferably the following device: PHILIPS PW1820.
  • the evaluation is preferably carried out by means of the analysis software X'Pert Pro MPD (PANalytical BV, Almelo, Netherlands).
  • the surface is determined according to Sonneveld & Visser.,
  • the reflexes are automatically identified by the program based on the selection of suitable PDF maps, (so far this is a semi-quantitative study). Then also done by means of the program automates the transformation into phases, the refinement of the dispersion in semi-automatic mode and then a Rietveld analysis.
  • the sintered shaped bodies of the calcium zirconium material according to the invention preferably have an open porosity of 5 to 50% by volume, preferably 8 to 40% by volume, determined in accordance with DIN EN 993-1: 1995-04.
  • the sintered shaped bodies in particular the sintered bricks, preferably have a bulk density of 2.50 to 4.50 g / cm 3 , in particular 2.60 to 4.30 g / cm 3 , determined in accordance with DIN 993-1: 1995 04 on.
  • the sintered shaped bodies are mechanically comminuted, preferably crushed and / or ground, for further processing after sintering, and then classified by sieving into particle size classes. Screening takes place in the sieve tower by dry screening according to DIN EN 933-1: 2012.
  • the screening machine Retsch AS 200 control at 0.5 mm amplitude for 2 min, used.
  • grain fraction or "grain class” means that no grains remain on the upper sieve and none fall through the lower sieve. So there is no oversize and no undersize. Grain classes thus each have grain sizes between the two specified test grain sizes.
  • the presynthesized granulation according to the invention has a very good thermomechanical resistance.
  • the granulation produced according to the invention preferably has a grain porosity (open porosity) according to DIN 66133: 1993 of 5 to 50% by volume, preferably 10 to 40% by volume, and / or preferably a mean pore diameter (dso) according to DIN 66133: 1993 from 0.5 to 2 pm, preferably 0.8 to 1, 2 pm, on.
  • the grain produced according to the invention preferably has a true density, determined by helium pycnometry according to DIN 66137-2: 2004 of 4.40 to 4.70 g / cm 3 , preferably from 4.65 to 4.70 g / cm 3 .
  • the granulation according to the invention can then be used in a conventional manner in coarse ceramic notches for the production of shaped or unshaped, coarse ceramic refractory products.
  • a coarse ceramic offset usually has a dry substance mixture of at least one refractory grain and, preferably, binder and / or water and / or liquid additives or additives. That is, the amount of binder (dry or liquid) and / or water and / or liquid additive is added additively and refers to the total dry mass of the dry material mixture (not to the total mass of the offset).
  • the liquid and / or solid or dry powdery binder and / or the liquid additive are preferably included in a separate container from the other dry components of the batch.
  • the binder is a binder suitable for refractory products, preferably a temporary binder. These binders are given for example in the Practical Guide, page 28 / point 3.2.
  • the additive is preferably a pressing aid.
  • the dry substance mixture has at least one coarse, presynthesized, calcium zirconium-containing grain having a particle size> 200 ⁇ m, preferably in an amount of from 10 to 90% by weight, preferably from 80 to 90% by weight, based on the total dry matter of the dry substance mixture, and / or at least one presynthesized, calcium zirconium-containing flour grain having a particle size ⁇ 200 ⁇ m, preferably in an amount of 0 to 30% by weight, preferably from 10 to 20% by weight based on the total dry matter of the dry substance mixture.
  • the grain sizes of the grains are determined by means of dry sieving according to DIN EN 933-1: 2012.
  • the dry substance mixture may also contain at least one flour-like Ca raw material component and at least one flour-like ZrO 2 raw material component, from which further calcium zirconate is formed in situ during firing of the product.
  • the raw material component and the Zr0 2 raw material component are therefore the raw material components indicated above.
  • the raw material components are preferably contained in an equimolar ratio in the dry material mixture to form a phase-pure calcium zirconate.
  • the dry substance mixture preferably comprises exclusively presensitized, calciumzirconate-containing grains according to the invention and optionally the at least one Ca raw material component and the at least one ZrO 2 raw material component, particularly preferably it consists thereof.
  • the dry substance mixture can also have at least one further coarse grain size with a grain size> 200 ⁇ m and / or at least one further flour grain size with a grain size ⁇ 200 ⁇ m from other conventional refractory materials.
  • the dry substance mixture may comprise at least one dry additive for refractory materials, preferably in a total amount of ⁇ 5% by weight and / or at least one dry additive for refractory materials, preferably in a total amount of ⁇ 5% by weight.
  • the dry additive is an additive suitable for refractory products. These additives are given for example in the Practical Guide, page 28 / point 3.3. They are used to improve the processability or deformability or to modify the structure of the products and thus to achieve special properties.
  • the particle size distribution of the coarse grain fraction of the dry substance mixture is preferably continuous.
  • the grain distribution of the total dry substance mixture is preferably continuous.
  • the coarse grain fraction serves in a conventional manner as a supporting grain. From the proportion of flour grain, the binding matrix is formed during firing, in which the coarse grain fraction is embedded.
  • the offset according to the invention is used for the production of unshaped or shaped, heavy clay products.
  • a mixture or plastic mass is prepared from the dry mixture of the inventive offset with at least one liquid and / or solid binder and / or water and / or a pressing aid. If the offset contains a liquid binder and / or pressing aid, the addition of water is not necessary, but possible. But it can also be added only water. For optimal distribution of the binder (s) and / or the water and / or the pressing assistant, mixing is carried out, for example, for 3 to 10 minutes.
  • the mixture is poured into molds and pressed so that moldings are formed.
  • the pressing pressures are in common ranges, e.g. at 50 to 150 MPa, preferably at 100 to 150 MPa.
  • drying is carried out after pressing, e.g. between 40 and 110.degree. C., in particular between 100 and 105.degree.
  • the drying is preferably carried out to a residual moisture content of between 0 and 2% by weight, in particular between 0 and 1% by weight, determined in accordance with DIN 51078: 2002-12.
  • the dried, pressed stones can be used unfired or burned.
  • the pressed, preferably dried, pressed bricks in a ceramic kiln e.g. a tunnel kiln, ceramically fired, preferably between 1200 and 1800 ° C, in particular between 1400 and 1700 ° C.
  • a ceramic kiln e.g. a tunnel kiln
  • it is oxidatively fired, but depending on the material composition, a reducing fire may also be advantageous.
  • the shaping of the molded products can also be carried out in other conventional ways, preferably by slip casting or extrusion or extrusion of a plastic mixture or manual or mechanical ramming.
  • the mixture is correspondingly flowable.
  • the fired, shaped products, in particular the bricks preferably have a bulk density of 4.00 to 4.70 g / cm 3 , in particular 4.40 to 4.60 g / cm 3 , determined in accordance with DIN 993-1: 1995- 04 on.
  • the cold bending strength according to DIN EN 993-6: 1995-04 of the fired, shaped products according to the invention, in particular of the stones, is preferably from 10 to 40 MPa.
  • the fired, shaped products according to the invention in particular the stones, preferably have an E-modulus according to DIN EN ISO 12680-1: 2007-05 of 80 to 200 GPa, preferably 90 to 120 GPa.
  • a mixture of the dry material mixture according to the invention with at least one dry and / or liquid binder and / or water and / or at least one liquid additive is also prepared and the Mix eg placed behind a formwork. If the offset contains a liquid binder and / or admixture, the addition of water is not necessary, but possible. But it can also be added only water.
  • VI M titanium casting / titanium alloy crucibles
  • crucibles for other non-ferrous metals e.g., nickel base alloys
  • Table 1 shows an example of a composition for the production of a molding compound.
  • Calcium carbonate PreCarb 400 from Shufer Kalk GmbH & Co. KG, Diez and monoclinic zirconium dioxide (ZirPro CS02) from Saint-Gobain, Le Pontet Cedex, France, were used. used.
  • Table 1 Composition for the preparation of a molding compound
  • the dry raw materials were weighed and placed in an intensive mixer. After a mixing of 10 minutes, the water was added. The mixer was operated in countercurrent mode (whirler and plate rotate in different directions). The wet mass was mixed for a further 10 minutes. The resulting mass was then poured into the press recess of the hydraulic press. With a compression pressure of up to 50 MPa moldings have been pressed. After demolding, the drying was carried out at 100 ° C for 24 h. After that, the Samples sintered at 1400 ° C for 5 h, with a hold time during the ramp-up phase of 2 h at 900 ° C. The heating rate was 3 K min -1 . The cooling in the oven was free.
  • the material thus obtained was coarsely pre-shredded and then broken in a jaw crusher in different grain classes and then classified. Examination in the XRD showed only peaks attributable to CaZrO 3 (see FIG. 1). The material thus contained 100% CaZrO 3.
  • Embodiment 2 Production of a Thermoshock- and Corrosion-Resistant Molded Body Based on the Phase-Pure Calcium Zirconate from Example 1 of Different Grain Density:
  • Table 2 below shows a composition for the production of a coarse-grained refractory shaped body of CaZrO 3 synthesized therefor.
  • Table 2 Composition for the preparation of a coarse-grained refractory shaped body of CaZrO 3 synthesized therefor
  • the dry raw materials were first weighed in, while it was filled from fine to coarse in the mixing vessel.
  • a ToniMix building material mixer from Toni Kunststoffprüfsysteme GmbH was used. The dry raw materials were mixed for 5 minutes. The binder was then added and everything mixed for a further 5 minutes. Thereafter, the molding was carried out in a hydraulic uniaxial press. At 150 MPa specimens were prepared. After a brief drying at 100 ° C for 4 h sintering was carried out at 1650 ° C for 6 h with a holding time in the start-up phase at 900 ° C for 2 h. The heating rate was 2 K min -1 . Table 3 shows selected properties of the material thus produced.

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Abstract

La présente invention concerne procédé de synthèse pour la préparation d'un matériau réfractaire, oxyde-céramique en CaZrO3, en particulier sous forme d'un produit grains réfractaire, de préférence réduit mécaniquement, en particulier concassé et/ou broyé, ainsi qu'un remblai et un produit réfractaire céramique grossier moulé ou non moulé contenant au moins un produit en grains réfractaire présynthétisé contenant du zirconate calcium.
EP18812125.5A 2017-12-01 2018-11-28 Procédé de synthèse pour la préparation d'un matériau contenant du zirconate de calcium ainsi que remblai et produit réfractaire céramique grossier pourvu d'un produit en grains présynthétisé contenant du zirconate calcium Pending EP3717439A1 (fr)

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DE102017128626.8A DE102017128626B4 (de) 2017-12-01 2017-12-01 Syntheseverfahren zur Herstellung eines calciumzirkonathaltigen Werkstoffes sowie Versatz und grobkeramisches feuerfestes Erzeugnis mit einer vorsynthetisierten calciumzirkonathaltigen Körnung und deren Verwendungen
PCT/EP2018/082904 WO2019106052A1 (fr) 2017-12-01 2018-11-28 Procédé de synthèse pour la préparation d'un matériau contenant du zirconate de calcium ainsi que remblai et produit réfractaire céramique grossier pourvu d'un produit en grains présynthétisé contenant du zirconate calcium

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CN115160002B (zh) * 2022-07-28 2023-08-29 中钢集团洛阳耐火材料研究院有限公司 一种碳化硅-锆酸钙复合耐火材料及其制备方法

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SU920048A1 (ru) 1979-12-21 1982-04-15 Харьковский Ордена Ленина Политехнический Институт Им.В.И.Ленина Способ получени плотного огнеупорного материала
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US5427722A (en) * 1993-06-11 1995-06-27 General Motors Corporation Pressure slip casting process for making hollow-shaped ceramics
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JP4534001B2 (ja) 2003-12-16 2010-09-01 独立行政法人物質・材料研究機構 ジルコニウム酸カルシウム粉末
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CN102001705A (zh) 2010-11-29 2011-04-06 江西晶安高科技股份有限公司 液相混合固相煅烧法合成锆酸钙工艺
DE102012003483B3 (de) 2012-02-21 2013-02-21 Technische Universität Bergakademie Freiberg Thermoschock- und korrosionsbeständiger Keramikwerkstoff auf der Basis von Calciumzirkonat und Verfahren zu seiner Herstellung
DE102012003478B4 (de) 2012-02-21 2015-08-06 Technische Universität Bergakademie Freiberg Verwendung eines oxidkeramischen Werkstoffes aus CaZrO3 als Auskleidungsmaterial für Vergasungsanlagen
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DE102017128626B4 (de) 2017-12-01 2024-06-06 Refratechnik Holding Gmbh Syntheseverfahren zur Herstellung eines calciumzirkonathaltigen Werkstoffes sowie Versatz und grobkeramisches feuerfestes Erzeugnis mit einer vorsynthetisierten calciumzirkonathaltigen Körnung und deren Verwendungen

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WO2019106052A1 (fr) 2019-06-06
RU2020112763A3 (fr) 2021-09-30
US20210171358A1 (en) 2021-06-10
DE102017128626B4 (de) 2024-06-06
RU2763197C2 (ru) 2021-12-28
ZA202001530B (en) 2021-03-31
CN111417609A (zh) 2020-07-14
RU2020112763A (ru) 2021-09-30

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